Abstract

Transfer cells are ubiquitous plant cells that play an important role in plant development as well as in responses to biotic and abiotic stresses. They are highly specialized and differentiated cells playing a central role in the acquisition, distribution and exchange of nutrients. Their unique structural traits are characterized by augmented ingrowths of invaginated secondary wall material, unsheathed by an amplified area of plasma membrane enriched in a suite of solute transporters. Similar morphological features can be perceived in vascular root feeding cells induced by sedentary plant-parasitic nematodes, such as root-knot and cyst nematodes, in a wide range of plant hosts. Despite their close phylogenetic relationship, these obligatory biotrophic plant pathogens engage different approaches when reprogramming root cells into giant cells or syncytia, respectively. Both nematode feeding-cells types will serve as the main source of nutrients until the end of the nematode life cycle. In both cases, these nematodes are able to remarkably maneuver and reprogram plant host cells. In this review we will discuss the structure, function and formation of these specialized multinucleate cells that act as nutrient transfer cells accumulating and synthesizing components needed for survival and successful offspring of plant-parasitic nematodes. Plant cells with transfer-like functions are also a renowned subject of interest involving still poorly understood molecular and cellular transport processes.

Highlights

  • The plant cell wall consists of a dynamic extracellular complex that responds to external and internal cellular signals, and forms a bridge between the plasma membrane and the cytoskeleton (Humphrey et al, 2007)

  • These strategies greatly depend on sophisticated cell wall modifications of the feeding site in order to transform vascular parenchymatic cells into transfer cells (TCs)

  • Nematode-induced syncytia or giant cells constitute a multinucleate model of TCs, and it is generally believed that wall protuberances arise as a result of nematode demand for nutrients

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Summary

Introduction

The plant cell wall consists of a dynamic extracellular complex that responds to external and internal cellular signals, and forms a bridge between the plasma membrane and the cytoskeleton (Humphrey et al, 2007). Concomitant with the structural modifications in a gall or a syncytium, cell walls thicken and finger-like protuberances (ingrowths or cell wall labyrinths) form (Schemes in Figures 1, 3 and 4; Berg et al, 2008; Sobczak et al, 2011; Vieira et al, 2013) with the function to increase the membrane surface area for solute uptake (e.g., Golinowski et al, 1996; Hussey and Grundler, 1998).

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